OneSource hiring MSAT and Technology Transfer professionals in Bengaluru for injectable manufacturing with salary upto 14 LPA.
The Indian pharmaceutical and CDMO industry is witnessing rapid growth, especially in the field of sterile injectable manufacturing and complex drug development. One of the fastest-growing names in this segment, OneSource, the contract development and manufacturing arm of Arcolab, has announced a major recruitment drive for MSAT & Technology Transfer professionals at its corporate office in Bengaluru.
If you are a pharma professional with hands-on experience in Technology Transfer, MSAT, injectable formulations, scale-up, and validation, this opportunity can significantly accelerate your career in a global CDMO environment. The company is inviting applications for the post of Executive / Senior Executive – MSAT & Technology Transfer.
Located on Bannerghatta Road, right opposite IIM Bangalore, this role offers exposure to advanced injectable manufacturing operations, global regulatory standards, and cross-functional collaboration with R&D, Manufacturing, QA, and Regulatory Affairs teams.
This detailed job post will give you complete information about the company, job responsibilities, qualifications, salary structure, growth opportunities, and the application process.
🟩 Key Highlight Box – OneSource MSAT & Technology Transfer Job 2025
- Company Name: OneSource (Arcolab)
- Job Location: Bengaluru (Bannerghatta Road, Opposite IIM Bangalore)
- Job Role: Executive / Senior Executive – MSAT & Technology Transfer
- Qualification Required: B.Pharm / M.Pharm / M.Sc
- Experience Required: 1 to 6 Years
- Industry Type: Pharmaceutical CDMO – Injectable Manufacturing
- Salary Package: ₹6 LPA to ₹14 LPA
- Job Type: Full-Time
- Application Mode: Email Application
- Working Domain: Sterile Injectables, Scale-up, Technology Transfer
- Job Status: Verified Job Opening
About OneSource (Arcolab)
OneSource is a rapidly expanding Contract Development and Manufacturing Organization (CDMO) that operates under Arcolab, a globally recognized pharmaceutical manufacturer. The organization is known for its advanced infrastructure, quality-driven culture, and strong presence in the injectable and parenteral drug manufacturing sector.
The company plays a crucial role in taking drug products from lab-scale development to commercial-scale production. With its strong MSAT and technology transfer framework, OneSource supports pharmaceutical innovators across the globe by ensuring smooth, compliant, and risk-controlled manufacturing transitions.
Working with OneSource means becoming part of a technical team that deals with high-complexity products, sterile manufacturing systems, international regulatory standards, and continuous process improvement programs.
About the MSAT & Technology Transfer Role
The Manufacturing Science and Technology (MSAT) function acts as the bridge between R&D and commercial manufacturing. The Technology Transfer team ensures that products developed at the laboratory or pilot scale are seamlessly transferred to large-scale production units with minimum risk, full documentation, and regulatory compliance.
At OneSource, the MSAT & Technology Transfer professional will be responsible for:
- Transferring newly developed injectable products into commercial manufacturing
- Supporting scale-up activities
- Executing validation batches
- Handling cross-site product transfers
- Coordinating with internal departments and external CMOs
This position is ideal for candidates who enjoy working in process engineering, regulatory documentation, validation support, and troubleshooting complex manufacturing issues.
Detailed Roles & Responsibilities
As an Executive / Senior Executive – MSAT & Technology Transfer, your responsibilities will include the following:
1. End-to-End Technology Transfer Management
You will be responsible for leading the complete technology transfer process of injectable products developed through in-house R&D. This includes:
- Transfer of formula, process parameters, and critical quality attributes
- Scale-up strategy preparation
- Process understanding and optimization
- Site readiness assessment for commercial production
2. Inter-Site and Third-Party Transfers
You will manage product transfers between:
- Internal manufacturing sites
- External CMOs and third-party manufacturers
This includes aligning documentation, quality standards, process parameters, and validation activities between sites.
3. Scale-Up and Exhibit Batch Execution
The role demands direct involvement in:
- Pilot-scale to commercial-scale batch execution
- Clinical, exhibit, and registration batch manufacturing
- Equipment qualification and process suitability checks
4. Documentation & Risk Management
You will prepare and review:
- Technology Transfer Protocols (TTP)
- Process Risk Assessments (FMEA, QbD studies)
- Gap Analysis Reports
- Manufacturing Instructions and Batch Records
Strict compliance with data integrity, SOPs, and regulatory standards is mandatory.
5. Regulatory Compliance
You must ensure product transfers align with:
- USFDA
- EU GMP
- MHRA
- WHO
- Other global regulatory expectations
You will also support regulatory submissions and product lifecycle management.
6. Cross-Functional Coordination
You will regularly collaborate with:
- Research & Development (R&D)
- Quality Assurance (QA)
- Regulatory Affairs (RA)
- Production & Engineering
Your role is to act as a technical bridge that ensures smooth communication and successful product commercialization.
7. Process Troubleshooting
During transfer and post-transfer stages, you will:
- Identify process deviations
- Investigate root causes
- Implement corrective and preventive actions
You will also support continuous improvement programs.
8. Process Validation & CPV Support
You will support:
- Process Qualification (PQ)
- Continued Process Verification (CPV)
- Ongoing process robustness studies
Educational Qualification & Experience Required
Required Educational Qualification:
Candidates must hold one of the following degrees:
- B.Pharm
- M.Pharm
- M.Sc (Pharmaceutics, Chemistry, or related discipline)
Additional qualifications such as MBA, Six Sigma, or Lean Manufacturing certifications will be considered a strong advantage.
Experience Criteria:
- Minimum: 1 Year
- Maximum: 6 Years
- Relevant hands-on experience in MSAT, Technology Transfer, Scale-Up, or Validation is mandatory.
Preferred Background:
- Injectable formulations such as vials, pre-filled syringes, cartridges, and lyophilized products
- Experience working with pharma manufacturing units or reputed CDMOs
- Familiarity with electronic systems such as TrackWise, SAP, and LIMS
- Strong understanding of QbD, PAT, and global regulatory standards
Skills Required for MSAT & Technology Transfer Professionals
To succeed in this role, candidates should possess:
- Strong technical knowledge of injectable manufacturing
- Excellent documentation and regulatory writing skills
- Problem-solving and analytical mindset
- Strong coordination and communication ability
- Hands-on experience with manufacturing deviations, investigations, and validation
- Knowledge of scale-up challenges and equipment qualification
Salary Structure & Employee Benefits
OneSource is offering a highly competitive salary package and an attractive benefits program:
- Annual CTC: ₹6 LPA to ₹14 LPA (based on experience and current CTC)
- Performance-linked incentives
- Annual bonus
- Group medical insurance
- Gratuity and provident fund
- Cab facility for employees
- Subsidized meals
- Modern manufacturing workplace
- Strong learning and development programs
- Fast-track career growth
Career Growth & Future Opportunities
Joining OneSource’s MSAT & Technology Transfer team provides significant long-term career advantages:
- Exposure to global injectable manufacturing projects
- Opportunity to work with international regulatory audits
- Hands-on experience with complex pharmaceutical products
- Cross-functional and cross-site technical leadership
- Career growth into MSAT Manager, Technical Lead, Validation Head, or Technology Transfer Lead roles
This is an excellent opportunity for professionals who want to build a long-term career in pharma manufacturing science and process engineering.
Job Location Details
- Office Location: OneSource Corporate Office
- Area: Bannerghatta Road
- Landmark: Opposite IIM Bangalore
- City: Bengaluru, Karnataka
This location offers excellent connectivity and access to major pharma and biotech hubs in Bengaluru.
Why You Should Apply for This Job
- Work with a fast-growing CDMO brand
- Be part of a high-impact injectable manufacturing team
- Competitive salary with strong learning curve
- Exposure to regulated markets such as US and EU
- Stable corporate structure with long-term growth
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✅ How to Apply for OneSource MSAT & Technology Transfer Job
Interested and eligible candidates can apply directly through email application as mentioned below:
- Email ID:
deepikag.rao@arcolab.com - Subject Line (Mandatory):
OneSource – Technology Transfer/MSAT - Documents to Attach:
- Updated Resume (PDF format preferred)
- Current CTC details
- Expected Salary
- Notice Period
Candidates are advised to mention their total years of experience in MSAT / Technology Transfer and injectable exposure clearly in the resume.
Early applicants will be given preference as shortlisting is expected to happen on a rolling basis.
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Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
